FDAJune 5, 2024device

DxC 500 AU Clinical Chemistry Analyzer, REF C63520 is an automated chemistry analyzer that measures analytes in samples, in combination with appropriate reagents, calibrators, quality control (QC) material and other accessories. This system is for in vitro diagnostic use only.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

There are two software bug issues with the analyzer. Issue 1: When a dedicated rack is reserved for calibration, after a calibration test has been placed and completed, the same rack may be used to place both a patient order and a calibration order. When a patient sample and a non-barcoded calibrator tube is processed on the rack, the calibration result will be reported as a patient result. Issue 2: calibration with expired calibrator. They both may cause erroneous patient results, but the probability of serious adverse health consequences or death is unlikely.

What to do

FDA enforcement status: Ongoing

Brands named

beckman coulter mishima k kbeckmanbeckman coulter

UPCs

14987666545065

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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